Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pone.0004407
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dc.titleOscillations of the p53-Akt network: Implications on cell survival and death
dc.contributor.authorWee K.B.
dc.contributor.authorSurana U.
dc.contributor.authorAguda B.D.
dc.date.accessioned2020-03-18T05:52:15Z
dc.date.available2020-03-18T05:52:15Z
dc.date.issued2009
dc.identifier.citationWee K.B., Surana U., Aguda B.D. (2009). Oscillations of the p53-Akt network: Implications on cell survival and death. PLoS ONE 4 (2) : e4407. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0004407
dc.identifier.issn19326203
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/165605
dc.description.abstractIntracellular protein levels of p53 and MDM2 have been shown to oscillate in response to ionizing radiation (IR), but the physiological significance of these oscillations remains unclear. The p53-MDM2 negative feedback loop - the putative cause of the oscillations - is embedded in a network involving a mutual antagonism (or positive feedback loop) between p53 and AKT. We have shown earlier that this p53-AKT network predicts an all-or-none switching behavior between a pro-survival cellular state (low p53 and high AKT levels) and pro-apoptotic state (high p53 and low AKT levels). Here, we show that upon exposure to IR, the p53-AKT network can also reproduce the experimentally observed p53 and MDM2 oscillations. The present work is based on the hypothesis that the physiological significance of the experimentally observed oscillations could be found in their role in regulating the switching behavior of the p53-AKT network between pro-survival and pro-apoptotic states. It is shown here that these oscillations are associated with a significant decrease in the threshold levels of IR at which switching from a pro-survival to a pro-apoptotic state occurs. Moreover, oscillations in p53 protein levels induce higher levels of expression of p53-target genes compared to non-oscillatory p53, and thus influence cell-fate decisions between cell cycle arrest/ DNA damage repair versus apoptosis. © 2009 Wee et al.
dc.publisherPublic Library of Science
dc.sourceUnpaywall 20200320
dc.subjectmessenger RNA
dc.subjectphosphatidylinositol 3,4,5 trisphosphate 3 phosphatase
dc.subjectprotein BAD
dc.subjectprotein Bax
dc.subjectprotein bcl 2
dc.subjectprotein kinase B
dc.subjectprotein MDM2
dc.subjectprotein p53
dc.subjectapoptosis
dc.subjectarticle
dc.subjectcell cycle arrest
dc.subjectcell fate
dc.subjectcell survival
dc.subjectcomputer simulation
dc.subjectDNA damage
dc.subjectDNA repair
dc.subjectgene expression
dc.subjectgene function
dc.subjectgene targeting
dc.subjectionizing radiation
dc.subjectoscillation
dc.typeArticle
dc.contributor.departmentPHARMACOLOGY
dc.contributor.departmentPHYSIOLOGY
dc.description.doi10.1371/journal.pone.0004407
dc.description.sourcetitlePLoS ONE
dc.description.volume4
dc.description.issue2
dc.description.pagee4407
dc.published.statePublished
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